Canonical Allele Identifier: CA421737910

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169499000T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529762T>G , CM000663.2:g.169529762T>G	GRCh38
NC_000001.10:g.169499000T>G , CM000663.1:g.169499000T>G	GRCh37
NC_000001.9:g.167765624T>G	NCBI36
NG_011806.1:g.61770A>C , LRG_553:g.61770A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5265A>C MANE Select	ENSP00000356771.3:p.Ile1755=
ENST00000367796.3:c.5280A>C	ENSP00000356770.3:p.Ile1760=
ENST00000367797.7:c.5265A>C	ENSP00000356771.3:p.Ile1755=
NM_000130.4:c.5265A>C , LRG_553t1:c.5265A>C	NP_000121.2:p.Ile1755=
XM_017000660.2:c.4854A>C	XP_016856149.1:p.Ile1618=
NM_000130.5:c.5265A>C MANE Select	NP_000121.2:p.Ile1755=